Parikh P, Powles R, Treleaven J, Helenglass G, Gore M, Rose M, Talbot D, Milan S, Smith C, Pinkerton R
Department of Medicine, Royal Marsden Hospital, Sutton, Surrey, UK.
Br J Cancer. 1990 Nov;62(5):830-3. doi: 10.1038/bjc.1990.387.
In a single centre, 52 newly diagnosed patients with acute myeloid leukemia (AML) under the age of 56 years received induction chemotherapy commencing with high-dose cytosine arabinoside (Ara-C) and etoposide (Protocol BF11), followed by Ara-C, 6 thioguanine (6TG). A total of 67% of patients entered remission using these drugs. An anthracycline was added for those patients not in remission. The overall remission rate (CR) was 86.5% (45/52), with a minimum follow-up of 90 days. Patients are hospitalised for relatively short periods, and consequently require less blood product and antibiotic support. Patients in continuing first remission following induction with Ara-C and etoposide are similar in number to those in continuing first remission who initially received an anthracycline. This would imply that the efficiency of Ara-C and etoposide in inducing long-term disease-term survival is comparable with anthracycline-containing regimens. We conclude that high-dose Ara-C and etoposide used in the first induction cycle for treating AML have good antileukaemic effect with acceptable toxicity.
在一个中心,52例年龄在56岁以下新诊断的急性髓系白血病(AML)患者接受了以大剂量阿糖胞苷(Ara-C)和依托泊苷开始的诱导化疗(方案BF11),随后使用阿糖胞苷、6-硫鸟嘌呤(6TG)。使用这些药物,共有67%的患者进入缓解期。对于未缓解的患者加用了蒽环类药物。总缓解率(CR)为86.5%(45/52),最短随访时间为90天。患者住院时间相对较短,因此所需的血液制品和抗生素支持较少。接受阿糖胞苷和依托泊苷诱导后持续首次缓解的患者数量与最初接受蒽环类药物治疗后持续首次缓解的患者数量相似。这意味着阿糖胞苷和依托泊苷诱导长期疾病生存的效率与含蒽环类药物的方案相当。我们得出结论,用于AML首次诱导周期的大剂量阿糖胞苷和依托泊苷具有良好的抗白血病效果,且毒性可接受。